127 related articles for article (PubMed ID: 26858800)
1. The Diversity of the Clinical Phenotypes in Patients With Fibrodysplasia Ossificans Progressiva.
Al Kaissi A; Kenis V; Ben Ghachem M; Hofstaetter J; Grill F; Ganger R; Kircher SG
J Clin Med Res; 2016 Mar; 8(3):246-53. PubMed ID: 26858800
[TBL] [Abstract][Full Text] [Related]
2. Early diagnosis of fibrodysplasia ossificans progressiva.
Kaplan FS; Xu M; Glaser DL; Collins F; Connor M; Kitterman J; Sillence D; Zackai E; Ravitsky V; Zasloff M; Ganguly A; Shore EM
Pediatrics; 2008 May; 121(5):e1295-300. PubMed ID: 18450872
[TBL] [Abstract][Full Text] [Related]
3. Clinical and Genetic Analysis of Fibrodysplasia Ossificans Progressiva: A Case Report and Literature Review.
Lakkireddy M; Chilakamarri V; Ranganath P; Arora AJ; Vanaja MC
J Clin Diagn Res; 2015 Aug; 9(8):RD01-3. PubMed ID: 26436010
[TBL] [Abstract][Full Text] [Related]
4. Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1.
Whyte MP; Wenkert D; Demertzis JL; DiCarlo EF; Westenberg E; Mumm S
J Bone Miner Res; 2012 Mar; 27(3):729-37. PubMed ID: 22131272
[TBL] [Abstract][Full Text] [Related]
5. The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call.
Towler OW; Shore EM; Xu M; Bamford A; Anderson I; Pignolo RJ; Kaplan FS
Eur J Med Genet; 2017 Jul; 60(7):399-402. PubMed ID: 28473268
[TBL] [Abstract][Full Text] [Related]
6. Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes.
Hasegawa K; Tanaka H; Futagawa N; Miyahara H; Tsukahara H
Case Rep Genet; 2022; 2022():5021758. PubMed ID: 36060212
[TBL] [Abstract][Full Text] [Related]
7. Fibrodysplasia ossificans progressiva in a 3-year-old female patient.
Moreira C; Dapueto G; Peluffo G; Vomero A; Tapié A; Rodríguez S; Raggio V; Suárez R; Giachetto G; García L
Bol Med Hosp Infant Mex; 2023; 80(1):69-73. PubMed ID: 36867574
[TBL] [Abstract][Full Text] [Related]
8. Fibrodysplasia ossificans progressiva (stone man syndrome): a case report.
Shah ZA; Rausch S; Arif U; El Yafawi B
J Med Case Rep; 2019 Dec; 13(1):364. PubMed ID: 31785620
[TBL] [Abstract][Full Text] [Related]
9. Fibrodysplasia Ossificans Progressiva: A Case Series with Radiologic Findings.
Malik I; Sharma SC; Padhiyar MA; Rawal N; Mukherjee M
J Orthop Case Rep; 2022 Nov; 12(11):9-13. PubMed ID: 37013240
[TBL] [Abstract][Full Text] [Related]
10. Late-onset fibrodysplasia ossificans progressiva with atypical presentation: A case report.
Cunningham CM; Royeca JM; King SW; Pandit H
Case Rep Womens Health; 2019 Jul; 23():e00134. PubMed ID: 31384566
[TBL] [Abstract][Full Text] [Related]
11. Difficult diagnosis and genetic analysis of fibrodysplasia ossificans progressiva: a case report.
Tian S; Zhu J; Lu Y
BMC Med Genet; 2018 Feb; 19(1):30. PubMed ID: 29482508
[TBL] [Abstract][Full Text] [Related]
12. The Developmental Phenotype of the Great Toe in Fibrodysplasia Ossificans Progressiva.
Towler OW; Kaplan FS; Shore EM
Front Cell Dev Biol; 2020; 8():612853. PubMed ID: 33364240
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of 20 years experience of fibrodysplasia ossificans progressiva in Iran: lessons for early diagnosis and prevention.
Raees-Karami SR; Jafarieh H; Ziyayi V; Shekarriz Foumani R; Aghighi Y
Clin Rheumatol; 2012 Jul; 31(7):1133-7. PubMed ID: 22526474
[TBL] [Abstract][Full Text] [Related]
14. Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva.
Kitterman JA; Kantanie S; Rocke DM; Kaplan FS
Pediatrics; 2005 Nov; 116(5):e654-61. PubMed ID: 16230464
[TBL] [Abstract][Full Text] [Related]
15. Natural history of fibrodysplasia ossificans progressiva: cross-sectional analysis of annotated baseline phenotypes.
Pignolo RJ; Baujat G; Brown MA; De Cunto C; Di Rocco M; Hsiao EC; Keen R; Al Mukaddam M; Sang KLQ; Wilson A; White B; Grogan DR; Kaplan FS
Orphanet J Rare Dis; 2019 May; 14(1):98. PubMed ID: 31053156
[TBL] [Abstract][Full Text] [Related]
16. Classical and atypical Fibrodysplasia Ossificans Progressiva in India.
Madhuri V; Santhanam M; Sugumar LK; Rajagopal K; Chilbule SK
Ann Hum Genet; 2015 Jul; 79(4):245-52. PubMed ID: 26058333
[TBL] [Abstract][Full Text] [Related]
17. Palovarotene Inhibits Heterotopic Ossification and Maintains Limb Mobility and Growth in Mice With the Human ACVR1(R206H) Fibrodysplasia Ossificans Progressiva (FOP) Mutation.
Chakkalakal SA; Uchibe K; Convente MR; Zhang D; Economides AN; Kaplan FS; Pacifici M; Iwamoto M; Shore EM
J Bone Miner Res; 2016 Sep; 31(9):1666-75. PubMed ID: 26896819
[TBL] [Abstract][Full Text] [Related]
18. A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family.
Fontaine K; Sémonin O; Legarde JP; Lenoir G; Lucotte G
Genet Couns; 2005; 16(2):149-54. PubMed ID: 16080294
[TBL] [Abstract][Full Text] [Related]
19. Fibrodysplasia ossificans progressiva with minor unilateral hallux anomaly in a sporadic case from Northern Tanzania with the common ACVR1c.617G>A mutation.
Saleh M; Commandeur J; Bocciardi R; Kinabo G; Hamel B
Pan Afr Med J; 2015; 22():299. PubMed ID: 26966495
[TBL] [Abstract][Full Text] [Related]
20. Fibrodysplasia Ossificans Progressiva in a Four year Old Child.
Kardile M; Nayak S; Nagaraja HS; Mishra AK
J Orthop Case Rep; 2012; 2(2):17-20. PubMed ID: 27298858
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
